RecruitingPhase 2NCT05424003

Randomized Double Blinded Placebo-Controlled w/Semaglutide to Prevent Weight Gain After Liver Transplant

A Randomized Double Blinded Placebo-Controlled Trial of Semaglutide to Prevent Weight Gain Following Liver Transplantation


Sponsor

Virginia Commonwealth University

Enrollment

50 participants

Start Date

Feb 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

In this study, semaglutide will be compared to placebo (a look-alike inactive substance, a "sugar pill") to determine if its use will prevent weight gain after liver transplantation (LT). In addition, researchers will be testing to determine if semaglutide prevents the development of Non-Alcoholic Fatty Liver Disease (NAFLD) after transplant through Magnetic Resonance Imaging (MRI) and laboratory results.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria9

  • Male or female age 18-75 years who received LT for any indication (i.e. NASH, hepatitis C, alcohol-induced cirrhosis, autoimmune hepatitis, etc.)
  • Liver transplant surgery within 8-24 weeks prior to randomization
  • Fasting glucose > 125 mg/dL or presence of diabetes (HbA1c≥6.5% or use of diabetes medications) or pre-diabetes (HbA1c >5.7%)
  • Ability to provide informed consent
  • Discharged from the hospital following LT surgery
  • Tolerating diet
  • Normal graft function* (determined by treating hepatologist/surgeon based on clinical status and hepatic panel)
  • Stable immunosuppression according the VCU (Virginia Commonwealth University) post-LT protocols ** (i.e. calcineurin inhibitors + mycophenolate)
  • Eligible female patients will be (1) non-pregnant, evidenced by a negative urine pregnancy test, (2) non-lactating, (3)surgically sterile or post-menopausal, or they will agree to continue to use an accepted method of birth control during the study

Exclusion Criteria14

  • BMI≤ 27kg/m2
  • GFR (Glomerular Filtration Rate) ≤ 25 ml/min/1.73m2
  • Type 1 autoimmune diabetes (by anti-GAD (glutamic acid decarboxylase) or history of ketoacidosis)
  • History of gastroparesis
  • Familial or personal history of medullary thyroid cancer or MEN (Multiple Endocrine Neoplasia) 2
  • History of pancreatitis
  • History of active malignancy post- LT with the exception of non-melanoma skin cancers
  • History of uncontrolled or unstable diabetic retinopathy or maculopathy
  • Acute cellular rejection
  • Hepatic artery thrombosis
  • Medical non-compliance
  • Active treatment with GLP (glucagon-like peptide)-1RA (receptor agonist) or SGLT (sodium-glucose cotransporter)-2 inhibitors at time of screening
  • History of hypersensitivity to semaglutide or its excipients
  • Women who are nursing, pregnant, or planning to become pregnant during the study, or are not using adequate contraceptive measures

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Interventions

DRUGSemaglutide Pen Injector

Starting dose of 0.24 mg injected weekly and increased every 4 weeks to a potential maximum dose of 2.4 mg weekly at 20 weeks followed by 52 weeks of weekly injections at the maximum tolerable dose

DRUGPlacebo

Placebo solution injected weekly for 72 weeks


Locations(1)

Virginia Commonwealth University

Richmond, Virginia, United States

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NCT05424003


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